57693-96-6

Upstream product

• 15731-13-2 {(CH₃)2N}2BMn{(CO)4P(C₆H₅)3} 
• 15279-67-1 dimanganese octacarbonyl di-(triphenyl phosphine) 
• 96-32-2 bromoacetic acid methyl ester 
• 14592-26-8 nonacarbonyl(triphenylphosphine)dimanganese 
• 14516-54-2 bromopentacarbonylmanganese(I) 
• 603-35-0 triphenylphosphine 
• 100-39-0 benzyl bromide 

Downstream Products

• 15662-31-4 mer,trans-BrMn(CO)3(PPh₃)2 
• 88666-22-2 cis-[Mn(CO)4(PPh₃)(CH₂OCH₃)] 
• 77438-16-5 (methoxycarbonylmethyl)tetracarbonyltriphenylphosphinemanganese 
• 54039-46-2 pentacarbonyl(triphenylphosphine)manganese tetrafluoroborate 
• 39796-96-8 cis-tetracarbonyl(triphenylphosphine)manganese hydride 
• 65035-20-3 (η5-1-bromoindenyl)tricarbonylmanganese(I) 
• 15614-85-4 fac-tricarbonylbromobis(triphenylphosphite)manganese(I) 
• 86619-62-7 fac-tricarbonyl(2-cyano-2-triphenylphosphoranylidenedithioacetato-S,S')(triphenylphosphine)manganese(I) 
• 906645-00-9 [Mn(CO)3(triphenylphosphine)(tetraphenyldiselenoimidophosphinato-κ2Se)] 
• 108486-76-6 {Mn(CO)4(P(C₆H₅)3)2}⁽¹⁺⁾*ClO₄^(1-)={Mn(CO)4(P(C₆H₅)3)2}{ClO₄} 
• 84430-58-0 fac-Tricarbonyl(triphenylphosphan)(triphenylstannandithiocarboxylato-S,S')mangan(I) 
• 103190-03-0 Mn(CO)3((C₆H₅)2PC(S)NCH₃)((C₆H₅)3P) 

Relevant academic research and scientific papers

Dichotomy of Manganese Catalysis via Organometallic or Radical Mechanism: Stereodivergent Hydrosilylation of Alkynes

Herein, we disclose the first manganese-catalyzed hydrosilylation of alkynes featuring diverse selectivities. The highly selective formation of E-products was achieved by using mononuclear MnBr(CO)5 with the arsenic ligand, AsPh3. Whereas using the dinuclear catalyst Mn2(CO)10 and LPO (dilauroyl peroxide) enabled the reversed generation of Z-products in good to excellent stereo- and regioselectivity. Such a way of controlling the reaction stereoselectivity is unprecedented. Mechanistic experiments revealed the dichotomy of manganese catalysis via organometallic and radical pathways operating in the E- and Z-selective routes, respectively.

Synthesis and structural studies of phosphorus carbonyl manganacycles containing the tetraphenyldiselenoimidodiphosphinato ligand

The [Mn(CO)4-x(L){Ph2P(Se)NP(Se)Ph2-κ 2Se}] complexes, where x = 1 for L = PPh3 and PMePh2, and x = 2 for L = Ph2PCH2CH2PPh2 (diphos), were synth

Photochemical reactions between dinuclear metal carbonyl complexes and alkyl halides. Formal oxidative addition across a metal-metal single bond proceeding by a free radical chain mechanism

Photochemical reactions between (L = CO, PBu3, PEt3, P(OMe)3, P(OPh)3, PPh3) and alkyl halides (RX) yield both alkyl and halo complexes, and , in equimolar quantities.Kinetic and quantum yield studies suggest that these reactions proceed by a radical chain pathway involving CO dissociation from the dinuclear complex and metal-metal bond homolysis of the coordinatively unsaturated dinuclear intermediate.

DARSTELLUNG UND EIGENSCHAFTEN VON ACETONYL-, PHENACYL- UND ACETOMETHOXY-MANGANCARBONYLVERBINDUNGEN. DIE KRISTALLSTRUKTUR VON ACETONYLTETRACARBONYLTRIPHENYLPHOSPHINMANGAN

Several oxoalkylpentacarbonylmanganese compounds RC(O)CH2Mn(CO)5 (R = Me, Ph, MeO) have been synthesized and investigated (IR, 1H NMR, mass spectra).They are thermo- and photo-labile and can be stabilized by triphenylphosphine substitution.Thus acetonylte